上海招聘

职位描述：
Chiltern is looking to recruit an experienced Clinical Research Associate (CRA) & Senior Clinical Research Associate with at least 2 years' CRA experiences or more, based in China.

Job Primary Functions:

? Prepare and conduct site visits including (but not limited to): qualification visits, initiation visits, monitoring visits, motivational visits, audit support visits, and close-out visits according to relevant SOPs, local requirements, the protocol and project plans as well as providing timely and comprehensive visit and status (i.e. patient recruitment) reports
? Communicate effectively with Chiltern Project Team members (i.e. Clinical Team Leader, Project Managers, Safety and Data Management) to ensure study completion per company and client requirements and timelines
? Proactively communicate with study sites and follow-up on all open issues in order to meet the project timelines. Ensure that all study-related documentation is tracked, printed, and filed as required by Chiltern SOPs, regulatory requirements, and other protocols
? To ensure that investigator site files are assembled appropriately and that all required documentation is in place, tracked and reconciled on a regular basis against the TMF files
? May support in mentoring less experienced CRAs on project or department tasks and requirements
? Perform other duties as required by the Department or Project Team

Job Qualifications:

? BSc or BA degree in a biomedical or related life science, or nursing qualification
? Previous CRA experience within clinical research of at least 1 or 2 years
? Good clinical knowledge with an understanding of medical terminology
? An understanding of the basics of physiology and pharmacology, and medical devices (when applicable)
? Understanding of the principles of ICH GCP and regulatory requirements
? Experience using a clinical trial management system
? Preferable experience using a clinical trial management system (CPMS)
? Experience as a CRA on single site and/or multicentre trials
? Good oral and written communication, organizational skills and personal presentation
? The ability to communicate effectively in Chinese and English

Additional Information:

? This is a permanent, full time role based in Shanghai or Beijing, and we also welcome homebased CRAs if the candidate is a senior or qualified staff.
Successful candidates will have the opportunity to be part of a growing company with a strong brand and professional employees that care about the work they are involved in. Chiltern is constantly working to develop training capacity, therapeutic expertise, new technologies and processes to be one of the leading CROs globally.

Working for Chiltern will offer an excellent opportunity to raise your profile and develop your career whilst giving you the flexibility to enjoy a good work life balance.

Please send your up-to-date CV to seoyoung.ahn@chiltern.com
Your interest will be treated in strict confidence.

Chiltern is a leading CRO that listens to client needs in order to customize solutions for the Biopharma industry. With a 32 year history, Chiltern delivers globally with therapeutic expertise in oncology, respiratory, anti-infectives / vaccines, ophthalmology and dermatology. Chiltern operates two specialty units: Chiltern Oncology is led by physicians, scientists and clinicians to uniquely manage all phases of hematologic and oncologic clinical drug development; and Chiltern Source is a world leader in tailored relationships for FSP, resourcing and staffing solutions. Chiltern’s 2,200 engaged professionals work across 45 countries to deliver flexible, responsive solutions that are “Designed Around You”.